Canonical Allele Identifier: PA2827722052
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 963725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Lys309Glu
CA398532989
NM_001353231.2:c.925A>G